Senior Method Development Analyst

Senior Method Development Analyst

Chemical Pharmaceuticals

Location Durham

Salary Negotiable based on Experience

Contract Permanent

Reference

Date Posted

Consultant

Apply now

4 weeks left to apply


CY Partners are currently looking to recruit an experienced Analytical Scientist on behalf of a North East based Pharmaceutical CDMO. This is a fantastic opportunity to join a company that is relatively young and growing and expanding into new and exciting areas and projects at this point in time.

If you are a Pharma Analyst with a strong technical ability and a dedicated forward thinking mindset looking to find a company where you can be more involved in the running of the department, the projects you work on and overall have a louder voice within the structure of the organisation, then this could be the role for you.

Responsibilities

  • The Senior Analyst will report directly to the Laboratory Operations Manager; this is a full-time position.
  • The Senior Analyst will primarily be involved in the development and validation of new methods of analysis for various pharmaceutical dosage forms.  However, some of the work will be routine analysis of stability samples to defined analytical methods.
  • All analysis will be carried out following the principles of GMP.
  • In addition to analysis, the Senior Analyst will be expected to carry out calibrations, performance equipment qualifications and maintenance, plus other tasks to ensure the smooth running of the laboratory.
  • The Senior Analyst will be expected to be familiar with all current Health and Safety requirements and to keep abreast of new developments in analytical chemistry.

Requirements

  • A minimum BSc degree in Chemistry, Pharmaceutical Science or equivalent
  • Extensive knowledge and practical experience in technologies used in the manufacture and testing of pharmaceutical products is necessary for this role.
  • Knowledge and extensive hands-on experience in the development and validation of HPLC, GC and IC
  • Knowledge and practical experience of GC-MS and Dissolution would also be an advantage.
  • Experience of working in a GMP environment having expert knowledge in pharmaceutical quality and regulatory requirements is essential for this role
  • Strong technical, communication and administrative skills to produce good quality documents, retain accurate records and to present data.
  • Experience in working within a team to plan and conduct work and solve problems is essential.
  • The candidate should be familiar with personal computing and be able to utilise spreadsheets, statistical, graphical and word processing packages, and be able to write, formal, descriptive reports of their work.
  • Knowledge and experience in six-sigma tools and technical and the development and implementation of process improvements would be an advantage.

If you would like to find out more about this role, please contact Graham at CY Partners on 07851 246 834


Senior Method Development Analyst

Chemical Pharmaceuticals

Apply now

4 weeks left to apply

Quick Apply

Already a member?

Yes, send me relevant communications
I accept the terms and conditions and privacy policy of CY Partners.


Related Vacancies

Regulatory Associate

Life Sciences Pharmaceuticals

LocationHertfordshire

SalaryCompetitive

ContractContract

CY Partners have an exciting opportunity for a Regulatory Associate to come and join a leading global pharmaceutical, based at their site in Hertfordshire. As a Regulatory Associate you will assist in…

Data Integrity Specialist

Chemical Pharmaceuticals

LocationNewcastle upon Tyne

Salary£28,000 - £34,000

ContractPermanent

Are you a chemical analyst with experience of supporting site systems and data Integrity? If so, we have a great opportunity for further individual development and to join a leading pharmaceutical Contract…

Medical Device Regulatory Executive

Clinical Life Sciences Pharmaceuticals

LocationHertfordshire

SalaryCompetitive

ContractContract

CY Partners have an exciting opportunity for a Medical Device Regulatory Executive to join a leading global pharmaceutical company, based at their site in Hertford. As a Medical Device Regulatory Executive, you…